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G Scarlato

Showing results (11-20 of 302) with videos related to

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Lancet (London, England)|August 3, 1991
Motoneuron-disease-like disorder after ganglioside therapyG Scarlato, E Nobile-Orazio
Acta Neuropathologica. Supplementum|January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven casesG Pellegrini, G Scarlato, M Moggio
Journal of Neurology|April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophyG Valli, G Scarlato, M Contartese
Advances in Experimental Medicine and Biology|January 1, 1982
alpha-Ketoglutarate induced transamination during ischemic exerciseC Cerri, F Fici, G Scarlato
Electromyography and Clinical Neurophysiology|January 1, 1983
Neurophysiological tests in human botulismG Valli, S Barbieri, G Scarlato
Journal of Neurology|January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parentsG Pellegrini, G Scarlato, M Moggio
Acta Neurologica|March 1, 1970
[Nosography of infantile and juvenile neurogenic amyotrophias in the light of histoenzymological studies]G Scarlato, F Cornelio, A Bollati
Journal of Neuropathology and Experimental Neurology|January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular diseaseG Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale|May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]G Scarlato, G Valli, G Meola
Acta Neurologica|July 1, 1974
[Histoenzymological particularities in a case of neuromyotonia]G Scarlato, R Schoenhuber, G Valli
Pageof 31

Showing results (11-20 of 302) with videos related to

Sort By:
Pageof 31
Lancet (London, England)|August 3, 1991
Motoneuron-disease-like disorder after ganglioside therapyG Scarlato, E Nobile-Orazio
Acta Neuropathologica. Supplementum|January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven casesG Pellegrini, G Scarlato, M Moggio
Journal of Neurology|April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophyG Valli, G Scarlato, M Contartese
Advances in Experimental Medicine and Biology|January 1, 1982
alpha-Ketoglutarate induced transamination during ischemic exerciseC Cerri, F Fici, G Scarlato
Electromyography and Clinical Neurophysiology|January 1, 1983
Neurophysiological tests in human botulismG Valli, S Barbieri, G Scarlato
Journal of Neurology|January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parentsG Pellegrini, G Scarlato, M Moggio
Acta Neurologica|March 1, 1970
[Nosography of infantile and juvenile neurogenic amyotrophias in the light of histoenzymological studies]G Scarlato, F Cornelio, A Bollati
Journal of Neuropathology and Experimental Neurology|January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular diseaseG Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale|May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]G Scarlato, G Valli, G Meola
Acta Neurologica|July 1, 1974
[Histoenzymological particularities in a case of neuromyotonia]G Scarlato, R Schoenhuber, G Valli
Pageof 31